chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	45732787	45732788	T	A	15	GENIC	homozygous	116931006
10	45732850	45732851	A	G	27	GENIC	homozygous	116931008
10	45733082	45733083	A	C	20	GENIC	homozygous	116931010
10	45733264	45733265	G	A	14	GENIC	homozygous	116584364
10	45733645	45733646	C	T	25	GENIC	homozygous	116931012
10	45733757	45733758	T	C	17	GENIC	homozygous	116931014
10	45733893	45733894	T	A	25	GENIC	homozygous	116584366
10	45734021	45734022	G	A	27	GENIC	homozygous	116931016
10	45734024	45734025	G	A	29	GENIC	homozygous	116931018
10	45734106	45734107	T	C	18	GENIC	heterozygous	117993381
10	45734221	45734222	C	T	26	GENIC	homozygous	116931020
10	45734270	45734271	G	A	22	GENIC	homozygous	116931022
10	45734362	45734363	C	T	22	GENIC	homozygous	116931024
10	45734897	45734898	A	G	23	GENIC	homozygous	116584370
10	45734898	45734899	A	C	24	GENIC	homozygous	116584372
10	45735035	45735036	G	A	32	GENIC	homozygous	116931026
10	45735373	45735374	T	C	34	GENIC	homozygous	116584374
10	45735441	45735442	G	A	28	GENIC	homozygous	116584376
10	45735728	45735729	C	T	29	GENIC	homozygous	116584378
10	45735734	45735735	A	C	26	GENIC	homozygous	116584380
10	45736949	45736950	A	C	34	GENIC	homozygous	116584382
10	45737121	45737122	A	G	34	GENIC	homozygous	116584384
10	45740159	45740160	C	G	26	GENIC	homozygous	116584386
10	45740205	45740206	G	A	38	GENIC	homozygous	116931028
10	45741241	45741242	T	C	21	GENIC	homozygous	116584388
10	45741874	45741875	C	T	26	GENIC	homozygous	116584390
10	45743122	45743123	G	A	37	GENIC	homozygous	116584392
10	45744081	45744082	T	A	30	GENIC	homozygous	116584394
10	45745081	45745082	A	G	33	GENIC	homozygous	116584396
10	45745645	45745646	T	C	33	GENIC	homozygous	116931030
10	45746312	45746313	G	A	38	GENIC	homozygous	116584398
10	45747291	45747292	G	T	28	GENIC	possibly homozygous	116877326